CHLORODIPHENYLPHOSPHINE

PRODUCT IDENTIFICATION

CAS NO 1079-66-9

CHLORODIPHENYLPHOSPHINE

EINECS NO. 214-093-2
FORMULA (C6H5)2PCl
MOL WT. 220.64
H.S. CODE

2931.00

TOXICITY  
SYNONYMS

Diphenyl Chlorophosphine; Diphenyl Phosphinous Chloride;

Diphenyl phosphine chloride; Diphenylchlorophosphine;  

PRICE

U$45/kg (200kgs)

CLASSIFICATION

ORGANOPHOSPHINES /

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE

clear to yellow liquid

MELTING POINT

14 - 16 C

BOILING POINT 320 C
SPECIFIC GRAVITY

1.18 - 1.20

SOLUBILITY IN WATER Violently reacts
pH  
VAPOR DENSITY 7.6

AUTOIGNITION

320 C

NFPA RATINGS

 

REFRACTIVE INDEX

1.634 - 1.637
FLASH POINT

138 C

STABILITY Stable under ordinary conditions

GENERAL DESCRIPTION & APPLICATIONS

Phosphine, also called Hydrogen Phosphide, PH3, is a colourless, poisonous, spontaneously flammable gas, with a disagreeable, garlic-like odour; melting point -133.5 C, boiling point -87.4 C. Phosphine is manufactured by the hydrolysis of metal phosphides, by the electrolysis of phosphorus in the presence of hydrogen, or by the phosphorus-steam reaction. Phosphine has the structure of ammonia (NH3) but with phosphorus in place of nitrogen. It is slightly soluble in cold water and soluble in alcohol. Phosphine is less soluble in water than ammonia. Phosphine is used in the synthesis of organophosphines and phosphonium derivatives and as a dopant in the manufacture of semiconductors. Aluminium or magnesium phosphide are used in the formulation for fumigation in pest control, and zinc phosphide is used as a rodenticide. Phophene is a starting material for the preparation of pesticides and flame retardants. Organophosphines are used as solvents for the extraction and separation processes, flame retardants, and in formulating fumigants and electronics applications of semiconductor manufacturing. Tertiary alkylphosphines act as chemical intermediate and catalyst in the production of industrial acids, alcohols, flavors & fragrances, and pharmaceuticals. Phosphonium describes a univalent radical, PH4. Quaternary phosphonium salts, obtained from tertiary alkylphosphines with the treatment with alkyl or aromatic halides, are replacing phase transfer catalysts and biocides functions for quaternary ammonium salts due to more effective performance and higher thermal stability. Phosphonium salts are used as epoxy curing agents. A variety of phosphine transition metal complexes including chiral complexes are synthesized as the very reactive and versatile homogeneous catalysts and stereospecific as well. Chlorodiphenylphosphine is used as an intermediate to make antioxidants, flame retardants, stabilizers, pesticides, catalysts, photoinitiators, and optical brighteners. It is used as a halogenation reagent for the conversion of alcohols into halides. It is used in the preparation of solid-phase reagent for the conversion of alcohols to alkyl halides.

SALES SPECIFICATION

APPEARANCE

clear to yellow liquid

CONTENT

97.0% min

TRANSPORTATION
PACKING  
HAZARD CLASS 8 (Packing Group: II)
UN NO. 3265
OTHER INFORMATION
Hazard Symbols: C, Risk Phrases: 14-29-34, Safety Phrases: 8-25-30-36/37/38-45